Canonical Allele Identifier: CA784479043

Gene: BANK1

Linked Data

• dbSNP Id: rs1401521587
• gnomAD v3: 4-101816146-C-CATTTGTT
• gnomAD v4: 4-101816146-C-CATTTGTT
• MyVariant Identifiers: chr4:g.102737303_102737304insATTTGTT (hg19) ; chr4:g.101816146_101816147insATTTGTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101816147_101816153dup , CM000666.2:g.101816147_101816153dup	GRCh38
NC_000004.11:g.102737304_102737310dup , CM000666.1:g.102737304_102737310dup	GRCh37
NC_000004.10:g.102956327_102956333dup	NCBI36
NG_015824.1:g.30541_30547dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.71-13661_71-13655dup MANE Select	ENSP00000320509.4:n.71-13661_71-13655dup
ENST00000322953.8:c.71-13661_71-13655dup	ENSP00000320509.4:n.71-13661_71-13655dup
ENST00000428908.5:c.70+25197_70+25203dup	ENSP00000412748.1:n.70+25197_70+25203dup
ENST00000444316.2:c.-21+2209_-21+2215dup	ENSP00000388817.2:n.-21+2209_-21+2215dup
ENST00000504592.5:c.26-13661_26-13655dup	ENSP00000421443.1:n.26-13661_26-13655dup
ENST00000508653.5:c.70+25197_70+25203dup	ENSP00000422314.1:n.70+25197_70+25203dup
NM_001083907.2:c.-21+2209_-21+2215dup	NP_001077376.2:n.-21+2209_-21+2215dup
NM_001127507.2:c.70+25197_70+25203dup	NP_001120979.2:n.70+25197_70+25203dup
NM_017935.4:c.71-13661_71-13655dup	NP_060405.4:n.71-13661_71-13655dup
XM_017008337.2:c.-20-13661_-20-13655dup	XP_016863826.1:n.-20-13661_-20-13655dup
NM_017935.5:c.71-13661_71-13655dup MANE Select	NP_060405.5:n.71-13661_71-13655dup
NM_001083907.3:c.-21+2209_-21+2215dup	NP_001077376.3:n.-21+2209_-21+2215dup
NM_001127507.3:c.70+25197_70+25203dup	NP_001120979.3:n.70+25197_70+25203dup